Promoting 2D Growth in Colloidal Transition Metal
Sulfide Semiconductor Nanostructures via Halide Ions
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Abstract
Wet-chemically synthesized 2D transition
metal sulfides (TMS) are
promising materials for catalysis, batteries and optoelectronics,
however a firm understanding on the chemical conditions which result
in selective lateral growth has been lacking. In this work we demonstrate
that Ni<sub>9</sub>S<sub>8</sub>, which is a less common nonstoichiometric
form of nickel sulfide, can exhibit two-dimensional growth when halide
ions are present in the reaction. We show that the introduction of
halide ions reduced the rate of formation of the nickel thiolate precursor,
thereby inhibiting nucleation events and slowing growth kinetics such
that plate-like formation was favored. Structural characterization
of the Ni<sub>9</sub>S<sub>8</sub> nanoplates produced revealed that
they were single-crystal with lateral dimensions in the range of ∼100–1000
nm and thicknesses as low as ∼4 nm (about 3 unit cells). Varying
the concentration of halide ions present in the reaction allowed for
the shape of the nanostructures to be continuously tuned from particle-
to plate-like, thus offering a facile route to controlling their morphology.
The synthetic methodology introduced was successfully extended to
Cu<sub>2</sub>S despite its different growth mechanism into ultrathin
plates. These findings collectively suggest the importance of halide
mediated slow growth kinetics in the formation of nanoplates and may
be relevant to a wide variety of TMS